A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5519298



Internal ID295650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31636932..31637011hg38UCSC Ensembl
chr19:32127838..32127917hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv245n206
Supporting Variantsnssv17722770
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5519298
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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